Team Leader | Julphar
A well-known and well-reputed Company based in Ras al-Khaimah, United Arab Emirates is looking for an experienced, skilled, competent, mature, qualified, creative, and intelligent candidate with significant knowledge and relevant working experience for the position of “Team Leader”.
| Company Name | Julphar |
| Qualification | Bachelors Degree |
| Experience | 6- 8 years of Relevant Experience Required |
| Monthly Salary | 6,500 AED – 7,000 AED |
| Employment Type | Full Time | Permanent |
| Company Size | 50-100 Employees |
| Benefits | Medical Insurance |
| Location | Ras al-Khaimah |
We are hiring a creative Team Leader to join our all-star team at Julphar in Ras al-Khaimah.
Growing your career as a Full Time Team Leader is an awesome opportunity to develop productive skills.
If you are strong in project management, decision-making and have the right drive for the job, then apply for the position of Team Leader at Julphar today!
Job Title: Team Leader
Division: QUALITY CONTROL
Country: UNITED ARAB EMIRATES
Work Location: UAE (RAK head office)
Job Type: Team Leader Employment
Type: Full Time Employment (Limited Contract)
Job Description: Purpose: Provide analysis and processing of bulk, finished products or Raw Material on time by appropriate methods while respecting Good Manufacturing Practices. Support resolution of technical issues in the laboratory. First contact in case of analytical issue in the laboratory.
Key responsibilities & Accountability:
- Management of a Lab Team (12-18 staff for laboratory testing)
- Release of commercial lots, testing’s for stability studies
- Follow-up of the quality system used in the laboratory, trend and reagents follow-up …
- Responsibility of the laboratory and the follow-up of the equipment’s
- Critical review of analytical data
- Knowledge of deviation process is an asset
- Be a support to reach objectives targeted such as planning adherence.
- Manage Laboratories, Deviations, Investigation & CAPA and the resolution of technical issues in the laboratory.
- Act as Lead Investigator, take in charge analytical projects
- Train other technicians to the QC analysis Escalates problems effectively to QC Managers
- Equipment SME
- Perform double check of analytical tests to ensure the integrity of results
- Create SOPs and working documentation needed for QC laboratories
- GMP knowledge and experience to support the requirements expected by Swiss medic, European union agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system.
- Respect all GMP standards. GMP knowledge and experience to support the requirements expected by Swiss medic, European union agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system.
- Maintains records and ensures proper documentation of the analysis and enter data on SAP.
- Ensure the quality of results provided by the department
- Quality documentation writing (deviations, CAPA, procedures, protocols, reports …).
- Transversal interactions with other teams in QC, with QA and different MPU: Guarantee good communication for transversal interactions. Qualifications: – Education Bachelor of Science in Chemistry or Chemical Engineering or Pharmacy – Experience:
- Minimum 6 to 8 years’ experience in a Pharmaceutical Environment (Finished product , preferable )
- Proven process understanding (Pharma, GMP, investigation and method development)
- Continuous improvement experience (Lean, 5S, Problem Solving). – Training: Key Competencies:
- Safety, Quality, Result and Customer oriented
- Basic speaker (A2) English level
- Strong Team spirit. Demonstrate exemplarity behaviors.
- Leadership skills
- Open minded and flexible
- Work under pressure
- Excellent interpersonal and intrapersonal skills Technical Competencies:
Company Benefits
- Learning opportunities
- Opportunities to grow
- Competitive salary